Halmos Balazs, Rai Pragya, Min Jae, Hu Xiaohan, Chirovsky Diana, Shamoun Mark, Zhao Bin
Department of Oncology, Montefiore Medical Center/Albert Einstein College of Medicine, Bronx, NY, United States.
Center for Observational and Real-World Evidence, Merck & Co., Inc., Rahway, NJ, United States.
Front Oncol. 2024 Apr 18;14:1285280. doi: 10.3389/fonc.2024.1285280. eCollection 2024.
Front-line therapy with an EGFR tyrosine kinase inhibitor (TKI) is the standard of care for treating patients with advanced nonsquamous NSCLC with the common sensitizing exon 19 deletion and exon 21 L858R point mutations. However, EGFR TKI resistance inevitably develops. The optimal subsequent therapy remains to be identified, although platinum-containing chemotherapy regimens are often administered. Our objectives were to describe baseline characteristics, survival, and subsequent treatment patterns for patients with advanced nonsquamous NSCLC with exon 19 deletion or L858R mutation who received a platinum-based combination regimen after front-line EGFR TKI therapy.
This retrospective study used a nationwide electronic health record-derived deidentified database to select adult patients with advanced nonsquamous NSCLC, evidence of exon 19 deletion or L858R mutation, and ECOG performance status of 0-2 who initiated platinum-containing chemotherapy, with or without concomitant immunotherapy, from 1-January-2011 to 30-June-2020 following receipt of any EGFR TKI as first-line therapy or, alternatively, a first- or second-generation EGFR TKI (erlotinib, afatinib, gefitinib, dacomitinib) as first-line therapy followed by the third-generation EGFR TKI osimertinib as second-line therapy. Data cut-off was 30-June-2022. The Kaplan-Meier method was used to estimate overall survival (OS) after initiation of pemetrexed-platinum (n=119) or any platinum-based combination regimen (platinum cohort; n=311).
The two cohorts included two-thirds women (65%-66%) and 57%-58% nonsmokers; median ages were 66 and 65 years in pemetrexed-platinum and platinum cohorts, respectively. Median OS was 10.3 months (95% CI, 8.1-13.9) from pemetrexed-platinum initiation and 12.4 months (95% CI, 10.2-15.2) from platinum initiation; 12-month survival rates were 48% and 51%, respectively; 260 patients (84%) had died by the end of the study.
The suboptimal survival outcomes recorded in this study demonstrate the unmet need to identify more effective subsequent treatment regimens for patients with -mutated advanced nonsquamous NSCLC after EGFR TKI resistance develops.
表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKI)一线治疗是晚期非鳞状非小细胞肺癌(NSCLC)伴有常见敏感的外显子19缺失和外显子21 L858R点突变患者的标准治疗方案。然而,EGFR-TKI耐药不可避免地会出现。尽管含铂化疗方案经常被采用,但最佳的后续治疗方案仍有待确定。我们的目的是描述晚期非鳞状NSCLC伴有外显子19缺失或L858R突变患者在一线EGFR-TKI治疗后接受铂类联合方案的基线特征、生存率和后续治疗模式。
这项回顾性研究使用了一个全国性的源自电子健康记录的去识别数据库,以选择2011年1月1日至2020年6月30日期间开始接受含铂化疗(无论是否联合免疫治疗)、有外显子19缺失或L858R突变证据且东部肿瘤协作组(ECOG)体能状态为0-2的成年晚期非鳞状NSCLC患者,这些患者接受过任何EGFR-TKI作为一线治疗,或者作为一线治疗接受第一代或第二代EGFR-TKI(厄洛替尼、阿法替尼、吉非替尼、达可替尼),随后作为二线治疗接受第三代EGFR-TKI奥希替尼。数据截止日期为2022年6月30日。采用Kaplan-Meier方法估计培美曲塞-铂(n=119)或任何铂类联合方案(铂类队列;n=311)开始后的总生存期(OS)。
两个队列中三分之二为女性(65%-66%),57%-58%为非吸烟者;培美曲塞-铂队列和铂类队列的中位年龄分别为66岁和65岁。从开始使用培美曲塞-铂起的中位OS为10.3个月(95%CI,8.1-13.9),从开始使用铂类起的中位OS为12.4个月(95%CI,10.2-15.2);12个月生存率分别为48%和51%;到研究结束时,260例患者(84%)已经死亡。
本研究记录的次优生存结果表明,在EGFR-TKI耐药发生后,为伴有突变的晚期非鳞状NSCLC患者确定更有效的后续治疗方案这一需求尚未得到满足。